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XUV pump-XUV probe transient absorption spectroscopy at FELs.
Ding, Thomas; Rebholz, Marc; Aufleger, Lennart; Hartmann, Maximilian; Stooß, Veit; Magunia, Alexander; Birk, Paul; Borisova, Gergana Dimitrova; da Costa Castanheira, Carina; Rupprecht, Patrick; Mi, Yonghao; Gaumnitz, Thomas; Loh, Zhi-Heng; Roling, Sebastian; Butz, Marco; Zacharias, Helmut; Düsterer, Stefan; Treusch, Rolf; Ott, Christian; Pfeifer, Thomas.
Afiliación
  • Ding T; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Rebholz M; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Aufleger L; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Hartmann M; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Stooß V; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Magunia A; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Birk P; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Borisova GD; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • da Costa Castanheira C; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Rupprecht P; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Mi Y; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Gaumnitz T; Laboratorium für Physikalische Chemie, ETH Zürich, Vladimir-Prelog-Weg 2, 8093 Zürich, Switzerland.
  • Loh ZH; Division of Chemistry and Biological Chemistry, Division of Physics and Applied Physics, School of Physical and Mathematical Sciences, Nanyang Technological University, Singapore 637371, Singapore.
  • Roling S; Physikalisches Institut der Westfälischen Wilhelms-Universität Münster, Wilhelm-Klemm-Straße 10, 48149 Münster, Germany.
  • Butz M; Center for Soft Nanoscience, Busso-Peuss-Straße 10, 48149 Münster, Germany.
  • Zacharias H; Center for Soft Nanoscience, Busso-Peuss-Straße 10, 48149 Münster, Germany.
  • Düsterer S; Deutsches Elektronen-Synchrotron DESY, Notkestraße 85, 22607 Hamburg, Germany.
  • Treusch R; Deutsches Elektronen-Synchrotron DESY, Notkestraße 85, 22607 Hamburg, Germany.
  • Ott C; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
  • Pfeifer T; Max-Planck-Institut für Kernphysik, Saupfercheckweg 1, 69117 Heidelberg, Germany. christian.ott@mpi-hd.mpg.de thomas.pfeifer@mpi-hd.mpg.de.
Faraday Discuss ; 228(0): 519-536, 2021 May 27.
Article en En | MEDLINE | ID: mdl-33575691
ABSTRACT
The emergence of ultra-intense extreme-ultraviolet (XUV) and X-ray free-electron lasers (FELs) has opened the door for the experimental realization of non-linear XUV and X-ray spectroscopy techniques. Here we demonstrate an experimental setup for an all-XUV transient absorption spectroscopy method for gas-phase targets at the FEL. The setup combines a high spectral resolving power of E/ΔE ≈ 1500 with sub-femtosecond interferometric resolution, and covers a broad XUV photon-energy range between approximately 20 and 110 eV. We demonstrate the feasibility of this setup firstly on a neon target. Here, we intensity- and time-resolve key aspects of non-linear XUV-FEL light-matter interactions, namely the non-resonant ionization dynamics and resonant coupling dynamics of bound states, including XUV-induced Stark shifts of energy levels. Secondly, we show that this setup is capable of tracking the XUV-initiated dissociation dynamics of small molecular targets (oxygen and diiodomethane) with site-specific resolution, by measuring the XUV transient absorption spectrum. In general, benefitting from a single-shot detection capability, we show that the setup and method provides single-shot phase-locked XUV pulse pairs. This lays the foundation to perform, in the future, experiments as a function of the XUV interferometric time delay and the relative phase, which enables advanced coherent non-linear spectroscopy schemes in the XUV and X-ray spectral range.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Faraday Discuss Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Faraday Discuss Asunto de la revista: QUIMICA Año: 2021 Tipo del documento: Article